Highly Effective Chlorfenapyr+ Beta-Cyfluthrin (10%+5% Ec)

Chlorfenapyr 10% + Beta-cyfluthrin 5% EC

Chlorfenapyr NOMENCLATURE
Common name chlorfénapyr ((m) F-ISO); chlorfenapyr (BSI, E-ISO, ANSI) 
IUPAC name 4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile
Chemical Abstracts name 4-bromo-2-(4-chlorophenyl)-1-(ethoxymethyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile 
CAS RN [122453-73-0] 

Chlorfenapyr APPLICATIONS
Chlorfenapyr Biochemistry Oxidative removal in vivo of the N-ethoxymethyl group generates the active species, which is a mitochondrial uncoupler.

Chlorfenapyr Mode of action Insecticide and acaricide with mainly stomach and some contact action. Exhibits good translaminar, but limited systemic, activity in plants.

Chlorfenapyr Uses Control of many species of insects and mites, including those resistant to carbamate, organophosphate and pyrethroid insecticides and also chitin-synthesis inhibitors, in cotton, vegetables, citrus, top fruit, vines and soya beans. Among pests resistant to conventional products which are controlled by chlorfenapyr are Brevipalpus phoenicis (leprosis mite), Leptinotarsa decemlineata (Colorado potato beetle), Helicoverpa spp., Heliothis spp., Plutella xylostella (diamond-back moth) and Tetranychus spp. Also control of many species of structural and household Formicidae (especially Camponotus, Iridomyrmex, Monomorium and Solenopsis spp.), Blattellidae (especially Blatta, Blattella, Periplaneta and Supella spp.), Kalotermitidae (especially Incisitermes spp.) and Rhinotermitidae (especially Reticulitermes, Coptotermes and Heterotermes spp.), at use rates of between 0.125% to 0.50% a.i. w/w.

Chlorfenapyr Phytotoxicity No phytotoxicity observed at field use rates.

Beta-cyfluthrin NOMENCLATURE
Common name beta-cyfluthrin (BSI, E-ISO); bêta-cyfluthrine ((f) F-ISO); cyfluthrin-beta (Canada) 
IUPAC name a reaction mixture comprising two enantiomeric pairs: (S)-α-cyano-4-fluoro-3-phenoxybenzyl (1R,3R)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-4-fluoro-3-phenoxybenzyl (1S,3S)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate (II) with (S)-α-cyano-4-fluoro-3-phenoxybenzyl (1R,3S)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-4-fluoro-3-phenoxybenzyl (1S,3R)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate (IV) in ratio c. 1:2 Roth: A reaction mixture comprising two enantiomeric pairs (S)-α-cyano-4-fluoro-3-phenoxybenzyl (1R)-cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-4-fluoro-3-phenoxybenzyl (1S)-cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate (II) with (S)-α-cyano-4-fluoro-3-phenoxybenzyl (1R)-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-4-fluoro-3-phenoxybenzyl (1S)-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate (IV) in ratio c. 1:2
Chemical Abstracts name cyano(4-fluoro-3-phenoxyphenyl)methyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate 
CAS RN [68359-37-5] unstated stereochemistry; [86560-92-1] diastereoisomer (I); [86560-93-2] (II); [86560-94-3] (III); [86560-95-4] (IV) 

APPLICATIONS
Beta-cyfluthrin Biochemistry Acts on the nervous system of insects, and disturbs the function of neurons by interaction with the sodium channel.

Beta-cyfluthrin Mode of action Non-systemic insecticide with contact and stomach action. Acts on the nervous system, with rapid knockdown and long residual activity.

Beta-cyfluthrin Uses Insecticide effective against Lepidoptera, Coleoptera, Hemiptera and Homoptera on cotton, fruit, vegetables, cereals and other crops, at 7.5-20 g/ha. Also against migratory locusts and grasshoppers; and in animal health.

  Chlorfenapyr 10% + Beta-cyfluthrin 5% EC

Chlorfenapyr NOMENCLATURE
Common name chlorfénapyr ((m) F-ISO); chlorfenapyr (BSI, E-ISO, ANSI) 
IUPAC name 4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile
Chemical Abstracts name 4-bromo-2-(4-chlorophenyl)-1-(ethoxymethyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile 
CAS RN [122453-73-0] 

Chlorfenapyr APPLICATIONS
Chlorfenapyr Biochemistry Oxidative removal in vivo of the N-ethoxymethyl group generates the active species, which is a mitochondrial uncoupler.

Chlorfenapyr Mode of action Insecticide and acaricide with mainly stomach and some contact action. Exhibits good translaminar, but limited systemic, activity in plants.

Chlorfenapyr Uses Control of many species of insects and mites, including those resistant to carbamate, organophosphate and pyrethroid insecticides and also chitin-synthesis inhibitors, in cotton, vegetables, citrus, top fruit, vines and soya beans. Among pests resistant to conventional products which are controlled by chlorfenapyr are Brevipalpus phoenicis (leprosis mite), Leptinotarsa decemlineata (Colorado potato beetle), Helicoverpa spp., Heliothis spp., Plutella xylostella (diamond-back moth) and Tetranychus spp. Also control of many species of structural and household Formicidae (especially Camponotus, Iridomyrmex, Monomorium and Solenopsis spp.), Blattellidae (especially Blatta, Blattella, Periplaneta and Supella spp.), Kalotermitidae (especially Incisitermes spp.) and Rhinotermitidae (especially Reticulitermes, Coptotermes and Heterotermes spp.), at use rates of between 0.125% to 0.50% a.i. w/w.

Chlorfenapyr Phytotoxicity No phytotoxicity observed at field use rates.

Beta-cyfluthrin NOMENCLATURE
Common name beta-cyfluthrin (BSI, E-ISO); bêta-cyfluthrine ((f) F-ISO); cyfluthrin-beta (Canada) 
IUPAC name a reaction mixture comprising two enantiomeric pairs: (S)-α-cyano-4-fluoro-3-phenoxybenzyl (1R,3R)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-4-fluoro-3-phenoxybenzyl (1S,3S)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate (II) with (S)-α-cyano-4-fluoro-3-phenoxybenzyl (1R,3S)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-4-fluoro-3-phenoxybenzyl (1S,3R)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate (IV) in ratio c. 1:2 Roth: A reaction mixture comprising two enantiomeric pairs (S)-α-cyano-4-fluoro-3-phenoxybenzyl (1R)-cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-4-fluoro-3-phenoxybenzyl (1S)-cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate (II) with (S)-α-cyano-4-fluoro-3-phenoxybenzyl (1R)-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-4-fluoro-3-phenoxybenzyl (1S)-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate (IV) in ratio c. 1:2
Chemical Abstracts name cyano(4-fluoro-3-phenoxyphenyl)methyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate 
CAS RN [68359-37-5] unstated stereochemistry; [86560-92-1] diastereoisomer (I); [86560-93-2] (II); [86560-94-3] (III); [86560-95-4] (IV) 

APPLICATIONS
Beta-cyfluthrin Biochemistry Acts on the nervous system of insects, and disturbs the function of neurons by interaction with the sodium channel.

Beta-cyfluthrin Mode of action Non-systemic insecticide with contact and stomach action. Acts on the nervous system, with rapid knockdown and long residual activity.

Beta-cyfluthrin Uses Insecticide effective against Lepidoptera, Coleoptera, Hemiptera and Homoptera on cotton, fruit, vegetables, cereals and other crops, at 7.5-20 g/ha. Also against migratory locusts and grasshoppers; and in animal health.

 

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